US4632824A - Compositions applied in the mouth - Google Patents

Compositions applied in the mouth Download PDF

Info

Publication number
US4632824A
US4632824A US06/617,817 US61781784A US4632824A US 4632824 A US4632824 A US 4632824A US 61781784 A US61781784 A US 61781784A US 4632824 A US4632824 A US 4632824A
Authority
US
United States
Prior art keywords
tannic acid
teeth
protein
toothpaste
tooth
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US06/617,817
Inventor
Kazuo Hirota
Shoji Akahane
Kentaro Tomioka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GC Corp
Original Assignee
GC Dental Industiral Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by GC Dental Industiral Corp filed Critical GC Dental Industiral Corp
Assigned to G-C DENTAL INDUSTRIAL CORP., NO. 76-1, HASUNUMA-CHO, ITABASHI-KU, TOKYO JAPAN, A CORP. OF JAPAN reassignment G-C DENTAL INDUSTRIAL CORP., NO. 76-1, HASUNUMA-CHO, ITABASHI-KU, TOKYO JAPAN, A CORP. OF JAPAN ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: AKAHANE, SHOJI, HIROTA, KAZUO, TOMIOKA, KENTARO
Application granted granted Critical
Publication of US4632824A publication Critical patent/US4632824A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

  • the present invention relates generally to a composition used in the mouth which has a preventive effect on dental caries, and more particularly to a composition containing tannic acid derivatives being sparingly soluble to water.
  • compositions applied in the mouth refers to compositions used in the mouth, for instance, for dentifrices in the pastes, powders and gels, mouthwashes and gargles, oral refrigerants in the chewing gum, candy, liquid and pellet forms, caries preventive agents in the paste and liquid forms, tooth make-up agents and the like.
  • a dentifrice is a substance or preparation used with a toothbrush to aid mechanical cleaning of the accessible surfaces of the teeth.
  • a typical formulation for a dentifrice paste contains abrasives, flavoring mixture, humectants, thickening agents, foaming agents and water.
  • teeth reinforcing agents such as fluorides, enzyme inhibitor such as vitamin K and sodium N-lauroylsarcosine, germicidal agents such as hexylresorcin or nicotinnic acid amide have been used with the dentifrice compositions for the purpose of preventing tooth decay.
  • teeth reinforcing agents such as fluorides, enzyme inhibitor such as vitamin K and sodium N-lauroylsarcosine
  • germicidal agents such as hexylresorcin or nicotinnic acid amide have been used with the dentifrice compositions for the purpose of preventing tooth decay.
  • Such materials have both merits and demerits, and no utterly satisfactory materials are
  • the fluorides serve to reinforce teeth, but limitations are imposed upon the amount thereof in view of toxicity in vivo.
  • Sodium N-lauroylsarconsine produces a less stimulating action, is of low toxicity and has a strong fermentation preventive action, but is somewhat of a bitter taste and does not have sufficient antibacterial properties.
  • Recent studies have revealed that the traditional "tooth black" used previously in Japan serves to prevent dental caries.
  • the tooth black comprises a powder containing tannic acid as the main component and a solution containing ferrous acetate as the main component. The powder and the liquid are mixed and applied on the teeth.
  • tannic acid is found to serve to flocculate and astringe tooth protein, whereby tooth is reinforced, and to possess antibacterial and antienzymetic properties useful for the prevention of caries.
  • tannic acid easily undergoes coloration, especially blackens, so that it is aesthetically unpreferred. For that reason, extreme restriction is placed upon its use.
  • the wording "substance being sparingly soluble in water” used in the present disclosure refers to tannic acid derivatives which are hardly or slightly soluble in water, inter alia, tannic acid-protein combinations, tannic acid-formaldehyde combinations, acetyl tannic acid and metal tannates.
  • the protein used for the tannic acid-protein combinations may be of either simple or conjugated type.
  • simple protein such as protamin, globulin, albumin, glutelin, prolamin, gelatin and the like
  • conjugated protein such as nucleoprotein, phosphoprotein and the like.
  • albumin particular preference is given to albumin.
  • salts of tannic acid used in the present invention.
  • salts of low toxicity such as aluminium, calcium, zinc, magnesium and strontium salts.
  • Tannic acid derivatives can be added to the compositions applied in the mouth such as dentifrices, mouthwashes and gargles, oral refrigerants, caries preventive agents and tooth make-up agents etc.
  • a mouthwash is a solution for rinsing the teeth and mouth. Generally, a mouthwash serves as an adjunct in cleaning the mouth and as an aid in removing loose debris after brushing.
  • a gargle is liquid to wash mouth and throat especially for medicinal purposes.
  • An oral refrigerant is in such forms as chewing gum, candy, liquid and pellet etc. Chewing gum usually consists of a chicle base, glucose, powdered sugar, starch and flavoring. Other bases may be also used.
  • a caries preventive agent is an agent to have an effect on prevention of caries, for example, fluoride agents (fluoride solutions and gels, fluoride rinses, fluoride containing varnishes).
  • a tooth make-up agent is a kind of cosmetics applied on the teeth. This is similar to nail enamel, namely, it is tooth enamel.
  • compositions according to the present invention may contain other additives in addition to the tannic acid derivatives.
  • the incorporation of other known substances serving to prevent dental caries poses no problem.
  • tannic acid derivatives being sparingly soluble in water may be synthesized in various known processes.
  • Toothpaste was prepared by admixing together the following ingredients.
  • Dibasic calcium phosphate dihydrate 43.0% by weight
  • the obtained toothpaste underwent no discoloration after one-day storage.
  • Toothpaste was prepared by using the composition of Example 1, provided that 3.5% by weight of tannic acid was used in place of albumin tannate. After one-day storage, the resultant toothpaste apparently turned ashen.
  • Toothpaste was prepared by using the composition of Example 1 free from albumin tannate. After one-day storage, the resultant toothpaste underwent no discoloration.
  • the marrow was extracted from a fresh tooth pulled out of a cattle, which was in turn sterilized in an ethylene oxide gas sterilizer after ultrasonic washing.
  • a toothbrush manufactured by GC Dental Industrial Corp. and sold in the trade name of PROSPECK M
  • PROSPECK M to which 1.5 grams of the toothpaste of Example 1 were applied, was reciprocated 200 times for cleaning the surface of that tooth.
  • the thus cleaned tooth was suspended in mitis-salivarius liquid medium in which the overnight-cultured bacteria of streptococcus mutaos strains was planted at a concentration of 5%, and was then cultured at 37° C. for 8 hours under gentle stirring with a magnetic stirrer. Thereafter, the test piece was washed with water, dried under reduced pressure in a desiccator to observe the surface of enamel thereof with a scanning electron microscope (SEM).
  • SEM scanning electron microscope
  • Group A cleaned the teeth with a brush to which the toothpaste of Example 1, Groups B and C did so with brushes to which the toothpaste of Comparative Examples 1 and 2 was applied, and Group D did so with a dentifricefree brush.
  • Brushing was effected three times a day, say, in the morning, afternoon and evening, and continued for ten days. Brushing was then discontinued for 24 hours. Thereafter, the dirt was rubbed off from the neck of the entire upper jaw teeth located on the cheek with a ready-made applicator, planted in mitis-salivarius liquid medium, and allowed to stand at 37° C. for 48 hours.

Abstract

A composition applied in the mouth which has a preventive effect on dental carries and contains such tannic acid derivatives as of solubility resistance to water.

Description

FIELD OF THE INVENTION
The present invention relates generally to a composition used in the mouth which has a preventive effect on dental caries, and more particularly to a composition containing tannic acid derivatives being sparingly soluble to water.
BACKGROUND OF THE INVENTION
The wording "compositions applied in the mouth" used in the present disclosure refers to compositions used in the mouth, for instance, for dentifrices in the pastes, powders and gels, mouthwashes and gargles, oral refrigerants in the chewing gum, candy, liquid and pellet forms, caries preventive agents in the paste and liquid forms, tooth make-up agents and the like.
A dentifrice is a substance or preparation used with a toothbrush to aid mechanical cleaning of the accessible surfaces of the teeth. A typical formulation for a dentifrice paste contains abrasives, flavoring mixture, humectants, thickening agents, foaming agents and water. So far, teeth reinforcing agents such as fluorides, enzyme inhibitor such as vitamin K and sodium N-lauroylsarcosine, germicidal agents such as hexylresorcin or nicotinnic acid amide have been used with the dentifrice compositions for the purpose of preventing tooth decay. However, such materials have both merits and demerits, and no utterly satisfactory materials are still found. For instance, it is widely accepted that the fluorides serve to reinforce teeth, but limitations are imposed upon the amount thereof in view of toxicity in vivo. Sodium N-lauroylsarconsine produces a less stimulating action, is of low toxicity and has a strong fermentation preventive action, but is somewhat of a bitter taste and does not have sufficient antibacterial properties. Recent studies have revealed that the traditional "tooth black" used previously in Japan serves to prevent dental caries. The tooth black comprises a powder containing tannic acid as the main component and a solution containing ferrous acetate as the main component. The powder and the liquid are mixed and applied on the teeth. Among these, tannic acid is found to serve to flocculate and astringe tooth protein, whereby tooth is reinforced, and to possess antibacterial and antienzymetic properties useful for the prevention of caries. However, tannic acid easily undergoes coloration, especially blackens, so that it is aesthetically unpreferred. For that reason, extreme restriction is placed upon its use.
SUMMARY OF THE INVENTION
In consequence of intensive studies made of "the compositions applied in the mouth" which contain a substance having a preventive effect as is the case with tannic acid and undergoing no discoloration, it has unexpectedly been found that "the compositions applied in the mouth" containing tannic acid derivatives being sparingly soluble in water are best-suited for that purpose.
DETAILED DESCRIPTION OF THE INVENTION
The wording "substance being sparingly soluble in water" used in the present disclosure refers to tannic acid derivatives which are hardly or slightly soluble in water, inter alia, tannic acid-protein combinations, tannic acid-formaldehyde combinations, acetyl tannic acid and metal tannates.
The protein used for the tannic acid-protein combinations may be of either simple or conjugated type. For example, use may be made of simple protein such as protamin, globulin, albumin, glutelin, prolamin, gelatin and the like as well as conjugated protein such as nucleoprotein, phosphoprotein and the like. Of these protein, particular preference is given to albumin.
No particular limitation is placed upon the metal salts of tannic acid used in the present invention. However, it is preferred to make use of salts of low toxicity (in vivo) such as aluminium, calcium, zinc, magnesium and strontium salts.
Tannic acid derivatives can be added to the compositions applied in the mouth such as dentifrices, mouthwashes and gargles, oral refrigerants, caries preventive agents and tooth make-up agents etc. A mouthwash is a solution for rinsing the teeth and mouth. Generally, a mouthwash serves as an adjunct in cleaning the mouth and as an aid in removing loose debris after brushing. A gargle is liquid to wash mouth and throat especially for medicinal purposes. An oral refrigerant is in such forms as chewing gum, candy, liquid and pellet etc. Chewing gum usually consists of a chicle base, glucose, powdered sugar, starch and flavoring. Other bases may be also used. A caries preventive agent is an agent to have an effect on prevention of caries, for example, fluoride agents (fluoride solutions and gels, fluoride rinses, fluoride containing varnishes). A tooth make-up agent is a kind of cosmetics applied on the teeth. This is similar to nail enamel, namely, it is tooth enamel.
It is to be noted that the compositions according to the present invention may contain other additives in addition to the tannic acid derivatives. For instance, the incorporation of other known substances serving to prevent dental caries poses no problem.
It is also to be noted that the tannic acid derivatives being sparingly soluble in water, as used in the present invention, may be synthesized in various known processes.
The present invention will now be explained in further detail with reference to some examples, to which the invention is not limited.
EXAMPLE 1
Toothpaste was prepared by admixing together the following ingredients.
Dibasic calcium phosphate dihydrate: 43.0% by weight
Glycerin: 12.0
Albumin tannate: 3.5
Sorbitol: 10.0
Sodium carboxymethylcellulose: 0.9
Calcium silicate: 0.3
Sodium lauryl sulfate: 1.8
Distilled water: 27.3
Saccharin: 0.1
Perfume (of the peppermint type): 1.0
Butyl p-oxybenzoate: 0.1
The obtained toothpaste underwent no discoloration after one-day storage.
COMPARATIVE EXAMPLE 1
Toothpaste was prepared by using the composition of Example 1, provided that 3.5% by weight of tannic acid was used in place of albumin tannate. After one-day storage, the resultant toothpaste apparently turned ashen.
COMPARATIVE EXAMPLE 2
Toothpaste was prepared by using the composition of Example 1 free from albumin tannate. After one-day storage, the resultant toothpaste underwent no discoloration.
It was evidently appreciated from the Example 1, Comparative Example 1 and Comparative Example 2 that the toothpaste of Example 1 did not discolore unlike in Comparative Example 1.
EXPERIMENT 1
Plaque estimation was then made with the toothpaste of Example 1 and Comparative Examples 1 and 2.
The marrow was extracted from a fresh tooth pulled out of a cattle, which was in turn sterilized in an ethylene oxide gas sterilizer after ultrasonic washing. A toothbrush (manufactured by GC Dental Industrial Corp. and sold in the trade name of PROSPECK M), to which 1.5 grams of the toothpaste of Example 1 were applied, was reciprocated 200 times for cleaning the surface of that tooth. The thus cleaned tooth was suspended in mitis-salivarius liquid medium in which the overnight-cultured bacteria of streptococcus mutaos strains was planted at a concentration of 5%, and was then cultured at 37° C. for 8 hours under gentle stirring with a magnetic stirrer. Thereafter, the test piece was washed with water, dried under reduced pressure in a desiccator to observe the surface of enamel thereof with a scanning electron microscope (SEM).
In another experiment, SEM observation was carried out with a tooth sample which was cleaned in the same manner with a dentifrice-free brush.
In a further experiment, similar SEM observation was undertaken with a tooth sample cleaned with a brush to which albumin tannate-free dentifrice, for instance, those of Comparative Examples 1 and 2, was applied.
In consequence, it was observed that the surface of enamel of the tooth cleaned with the dentifrice-free brush was entirely covered with bacteria and plaque formed. On the contrary, 90% of enamel was covered with bacteria in the case of using the dentifrice of Comparative Example 2. It was also noted that 40% and 35% of enamel were covered with bacteria in the case of using the dentifrice formulations of Comparative Example 1 and Example 1, respectively. From this, it has been appreciated that albumin tannate has an effect upon the inhibition of plaque formation, which indicates that it serves to prevent dental caries.
EXPERIMENT 2
Twelve healthy men (23-29 old) were subdivided into four groups, each comprising three. Group A cleaned the teeth with a brush to which the toothpaste of Example 1, Groups B and C did so with brushes to which the toothpaste of Comparative Examples 1 and 2 was applied, and Group D did so with a dentifricefree brush. Brushing was effected three times a day, say, in the morning, afternoon and evening, and continued for ten days. Brushing was then discontinued for 24 hours. Thereafter, the dirt was rubbed off from the neck of the entire upper jaw teeth located on the cheek with a ready-made applicator, planted in mitis-salivarius liquid medium, and allowed to stand at 37° C. for 48 hours. Subsequently, the pH of the liquid medium was measured with a pH meter. The pH values of Groups A, B, C and D were respectively 6.2, 6.0, 5.6 and 5.2 on the average. It has been appreciated that Group A shows the lowest actvity to caries.

Claims (4)

What is claimed is:
1. In a method of treatment of teeth to prevent tooth decay of the surface of teeth on which Streptococcus mutans plaque causing dental caries forms, the improvement over traditional "tooth black", which blackens the teeth, which consists of the step of applying to said teeth a toothpaste, powder, gel, mouthwash, or gargle composition comprising a tannic acid derivative which is sparingly soluble in water, wherein said tannic acid derivative is selected from the group consisting of tannic acid--protein combinations, tannic acid--formaldehyde combinations and acetyl tannic acid in an amount effective to inhibit dental plaque formation.
2. The method of claim 1, wherein said tannic acid--protein combinations are made from a protein selected from the group consisting of protamin, globulin, albumin, glutelin, prolamin, gelatin, nucleoprotein and phosphoprotein.
3. The method of claim 2, wherein said protein is albumin.
4. The method of claim 5, further comprising application in a toothpaste containing dibasic calcium phosphate dihydrate.
US06/617,817 1983-06-06 1984-06-06 Compositions applied in the mouth Expired - Fee Related US4632824A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP58-99522 1983-06-06
JP58099522A JPS59225109A (en) 1983-06-06 1983-06-06 Composition for oral cavity application

Publications (1)

Publication Number Publication Date
US4632824A true US4632824A (en) 1986-12-30

Family

ID=14249563

Family Applications (1)

Application Number Title Priority Date Filing Date
US06/617,817 Expired - Fee Related US4632824A (en) 1983-06-06 1984-06-06 Compositions applied in the mouth

Country Status (4)

Country Link
US (1) US4632824A (en)
JP (1) JPS59225109A (en)
DE (1) DE3420337A1 (en)
GB (1) GB2141340B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5409692A (en) * 1990-03-30 1995-04-25 Suntory Limited Glucosyltransferase inhibitors, as well as dental caries prevention methods and anticarious foods using the same
US5843471A (en) * 1997-11-06 1998-12-01 Chaykin; Sterling Oral cleansing: methods and compositions
US5962550A (en) * 1997-03-19 1999-10-05 Gc Corporation Dental filling resin composition
US6197331B1 (en) 1997-07-24 2001-03-06 Perio Products Ltd. Pharmaceutical oral patch for controlled release of pharmaceutical agents in the oral cavity
US6217644B1 (en) 1998-08-09 2001-04-17 Gc Corporation Dental adhesive set
US6264472B1 (en) 1999-08-10 2001-07-24 Gc Corporation Method for setting dental glass ionomer cement
US6291548B1 (en) 1998-08-11 2001-09-18 Gc Corporation Dental cement composition
US20040131558A1 (en) * 2002-06-21 2004-07-08 Hauck Douglas J. Oral disease prevention and treatment
US20090062191A1 (en) * 2007-08-29 2009-03-05 Kiel Laboratories, Inc. Composition for maintaining gastrointestinal homeostasis

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101011049B1 (en) 2009-07-20 2011-01-25 김홍철 Oral composition which containing alpha hydroxy acid, and detal article comprising them
JP5461349B2 (en) * 2010-09-01 2014-04-02 株式会社イノアコーポレーション Method for producing polyphenol-containing protein

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1130566A (en) * 1964-10-20 1968-10-16 Carl Emanuel Allan Stralfors Dentifrice
US4022880A (en) * 1973-09-26 1977-05-10 Lever Brothers Company Anticalculus composition
JPS5438180A (en) * 1977-08-31 1979-03-22 Matsushita Electric Works Ltd Gas detector
US4146606A (en) * 1977-05-27 1979-03-27 Reiichi Yamaga Pharmaceutical compositions for dental use
GB2036750A (en) * 1978-11-23 1980-07-02 Payne M Tannin complexes
EP0028271A1 (en) * 1979-11-06 1981-05-13 Liau Weilin Dentifrice and its method of manufacture
US4273758A (en) * 1979-11-06 1981-06-16 Weilin Liau Dentifrice and its method of manufacture
EP0051752A2 (en) * 1980-11-12 1982-05-19 Weilin Liau Dentifrice, its method of manufacture and gargle
US4395398A (en) * 1980-04-02 1983-07-26 Bee Brand Medico Dental Co., Ltd. Dental hemostatic composition
US4524824A (en) * 1982-04-20 1985-06-25 G-C Dental Industrial Corporation Dental cement

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB454560A (en) * 1935-03-28 1936-09-28 Carl Heydenreich Tooth cleaning and thirst quenching preparation
GB1181079A (en) * 1967-03-03 1970-02-11 Vnii Chainoi Promy Colour Derived from Vegetable Raw Material and method of manufacturing the same
GB1290627A (en) * 1971-01-28 1972-09-27
GB1373001A (en) * 1971-01-28 1974-11-06 Unilever Ltd Anti-plaque and anti-calculus dentifrice
DE2657896C3 (en) * 1976-12-21 1979-12-06 Dobrivoje Dr. 8000 Muenchen Tomic Means with hemostatic and anti-inflammatory effects
CA1139229A (en) * 1979-06-20 1983-01-11 Thomas W. Ritchey Zinc salt with glycine in oral composition

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1130566A (en) * 1964-10-20 1968-10-16 Carl Emanuel Allan Stralfors Dentifrice
US4022880A (en) * 1973-09-26 1977-05-10 Lever Brothers Company Anticalculus composition
US4146606A (en) * 1977-05-27 1979-03-27 Reiichi Yamaga Pharmaceutical compositions for dental use
JPS5438180A (en) * 1977-08-31 1979-03-22 Matsushita Electric Works Ltd Gas detector
GB2036750A (en) * 1978-11-23 1980-07-02 Payne M Tannin complexes
EP0028271A1 (en) * 1979-11-06 1981-05-13 Liau Weilin Dentifrice and its method of manufacture
US4273758A (en) * 1979-11-06 1981-06-16 Weilin Liau Dentifrice and its method of manufacture
US4395398A (en) * 1980-04-02 1983-07-26 Bee Brand Medico Dental Co., Ltd. Dental hemostatic composition
EP0051752A2 (en) * 1980-11-12 1982-05-19 Weilin Liau Dentifrice, its method of manufacture and gargle
US4524824A (en) * 1982-04-20 1985-06-25 G-C Dental Industrial Corporation Dental cement

Non-Patent Citations (14)

* Cited by examiner, † Cited by third party
Title
Hirota et al, C.A. 102:84271z (1985). *
Kaya et al, C.A. 102:119416e (1985). *
Liao, C.A. 92:153171f (1980). *
Liau, C.A. 95:86334h (1981). *
Liau, C.A. 97:78711e (1982). *
Okuda, C.A. 98:221633j (1983). *
Payne, C.A. 94:82548n (1981). *
Stralfors, C.A. 66:103797g (1967). *
Stralfors, C.A. 70:22920x (1969). *
Sunstar, C.A. 101:216234f (1984). *
Sunstar, C.A. 93:173631e (1980). *
Teraoka, C.A. 90:132633b (1979). *
Weilin, C.A. 95:67823a (1981). *
Wrigley, C.A. 77:60323g (1972). *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5409692A (en) * 1990-03-30 1995-04-25 Suntory Limited Glucosyltransferase inhibitors, as well as dental caries prevention methods and anticarious foods using the same
US5962550A (en) * 1997-03-19 1999-10-05 Gc Corporation Dental filling resin composition
US6197331B1 (en) 1997-07-24 2001-03-06 Perio Products Ltd. Pharmaceutical oral patch for controlled release of pharmaceutical agents in the oral cavity
US5843471A (en) * 1997-11-06 1998-12-01 Chaykin; Sterling Oral cleansing: methods and compositions
US6013274A (en) * 1997-11-06 2000-01-11 Chaykin; Sterling Oral cleansing: methods and compositions
US6090402A (en) * 1997-11-06 2000-07-18 Chaykin; Sterling Oral cleansing: methods and compositions
US6217644B1 (en) 1998-08-09 2001-04-17 Gc Corporation Dental adhesive set
US6291548B1 (en) 1998-08-11 2001-09-18 Gc Corporation Dental cement composition
US6264472B1 (en) 1999-08-10 2001-07-24 Gc Corporation Method for setting dental glass ionomer cement
US20040131558A1 (en) * 2002-06-21 2004-07-08 Hauck Douglas J. Oral disease prevention and treatment
US20090062191A1 (en) * 2007-08-29 2009-03-05 Kiel Laboratories, Inc. Composition for maintaining gastrointestinal homeostasis
EP2065051A3 (en) * 2007-08-29 2009-07-15 Kiel Laboratories, Inc. Composition for maintaining gastrointestinal homeostasis comprising albumin and tannic acid

Also Published As

Publication number Publication date
JPS6216923B2 (en) 1987-04-15
DE3420337A1 (en) 1984-12-06
DE3420337C2 (en) 1988-08-11
GB8414259D0 (en) 1984-07-11
GB2141340A (en) 1984-12-19
GB2141340B (en) 1986-09-10
JPS59225109A (en) 1984-12-18

Similar Documents

Publication Publication Date Title
US5370863A (en) Oral care compositions containing hop acids and method
EP0173568B1 (en) Oral compositions
US5281410A (en) Methods of reducing plaque and gingivitis with reduced staining
US4550018A (en) Dental hygiene compositions
US6610276B2 (en) Multi-functional dental composition
JPS60233008A (en) Oral sanitary composition
US4545979A (en) Dental hygiene compositions
CA1237989A (en) Plaque disclosing agent
EP0008295A1 (en) Compositions and methods for inhibiting plaque formation
EP0278744B2 (en) Dentifrice composition for desensitising sensitive teeth
US4590061A (en) Antimicrobial plaque disclosing agent
CZ156795A3 (en) Mouth preparation containing agents against formation of microbial plaque, tartar, gingivitis and foetor ex ore
US4632824A (en) Compositions applied in the mouth
JPH04257511A (en) Antibacterial oral composition free from pollution
WO2020016713A1 (en) Amino acid containing oral care composition for treating caries by reducing lactic acid release in oral biofilms
US4477429A (en) Oral compositions comprising N.sup.α -alkyl derivatives of arginine
US4499068A (en) Oral compositions comprising NG -alkyl derivatives of arginine
US4477428A (en) Oral compositions comprising N.sup.α,NG -diacyl derivatives of arginine
WO1990015592A1 (en) Anti-plaque dentifrice
JP3783762B2 (en) Stain removal oral composition
JPH07267840A (en) Composition for oral cavity
JPH07133222A (en) Glucosyl transferase inhibitor
CN113710223B (en) Personal care compositions comprising piperlonglamide and methods of making the same
CN114096225B (en) Oral care compositions comprising Jiang Erchun and methods of making the same
RU2119328C1 (en) Toothpaste

Legal Events

Date Code Title Description
AS Assignment

Owner name: G-C DENTAL INDUSTRIAL CORP., NO. 76-1, HASUNUMA-CH

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:HIROTA, KAZUO;AKAHANE, SHOJI;TOMIOKA, KENTARO;REEL/FRAME:004607/0915

Effective date: 19840501

Owner name: G-C DENTAL INDUSTRIAL CORP., NO. 76-1, HASUNUMA-CH

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HIROTA, KAZUO;AKAHANE, SHOJI;TOMIOKA, KENTARO;REEL/FRAME:004607/0915

Effective date: 19840501

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Free format text: PAT HLDR NO LONGER CLAIMS SMALL ENT STAT AS INDIV INVENTOR (ORIGINAL EVENT CODE: LSM1); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
FP Lapsed due to failure to pay maintenance fee

Effective date: 19950104

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362